SG guided spinal Vs Blind spinal anaesthesia in obese patient
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/10/046144
- Lead Sponsor
- Government of Gujarat
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients eligible for surgery under subarachnoid block.
Patient posted for elective surgery.
Informed written consent
BMI >30.
Gender: Either
ASA physical status I and II
Exclusion Criteria
Patient refusing consent
Contraindication subarachnoid block,
Infection at the site of injection.
Bleeding and clotting disorders.
Patient receiving medication affecting coagulation.
Previous spine surgery or spine deformity.
� Patients with neurological abnormality.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)Time required to localise the mid-point of inter spinous space. <br/ ><br>2)Time required for identification of subarachnoid space (Free flow of CSF through spinal needle). <br/ ><br>3) Number of times needle redirected to obtained CSF (Number of passes). 4)The number of needle insertion attempts required to enter the subarachnoid space. <br/ ><br>5)Traumatic needle puncture. (Blood coming out through needle). <br/ ><br>Timepoint: Continuous time monitoring on a stopwatch in seconds from start of procedure to the end of procedure.
- Secondary Outcome Measures
Name Time Method 1)Peri procedural subjective pain score. <br/ ><br>2)Hemodynamic disturbance during procedure i.e. Tachycardia ,bradycardia,Hypertension,Hypotension,Arrythmia..Timepoint: All above parameters are observed at 1 min,5 min,10 min,15 min upto 30 min from start of procedure.